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rs60336366

From SNPedia

Orientationplus
Stabilizedplus
Make rs60336366(A;A)
Make rs60336366(A;G)
Make rs60336366(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position113650022
is asnp
is mentioned by
dbSNPrs60336366
ebirs60336366
HLIrs60336366
Exacrs60336366
Varsomers60336366
Maprs60336366
PheGenIrs60336366
hapmaprs60336366
1000 genomesrs60336366
hgdprs60336366
ensemblrs60336366
gopubmedrs60336366
geneviewrs60336366
scholarrs60336366
googlers60336366
pharmgkbrs60336366
gwascentralrs60336366
openSNPrs60336366
23andMers60336366
23andMe allrs60336366
SNP Nexus

SNPshotrs60336366
SNPdbers60336366
MSV3drs60336366
GWAS Ctlgrs60336366
Max Magnitude
GWAS snp
PMID [PMID 24939585]
Trait Age-related hearing impairment
Title Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Risk Allele
P-val 4E-6
Odds Ratio .27 [NR] unit increase